Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities.
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference2 articles.
1. the long arm of chromosome 4: further delineation of phenotypes;Lin, A.E.; Garver, K.L.; Diggans, G.;AmJ7 Med Genet,1988
2. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4;Beall, M.H.; Falk, R.E.; Ying, K.-L.;Am J Med Genet,1988
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1. Interstitial Deletion 4q due to a Complex Rearrangement Involving Chromosomes 1, 2, 4, 8, 14 and 16;Gazi Medical Journal;2018-07-01
2. 4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence ofKIThaploinsufficiency;American Journal of Medical Genetics Part A;2014-10-29
3. Array-based characterization of an interstitial de-novo deletion of chromosome 4q in a patient with a neuronal migration defect and hypocalcemia plus a literature review;Clinical Dysmorphology;2012-07
4. Case Report: Two newborns with chromosome 4 imbalances: deletion 4q33 → q35 and ring r (4) (pterq35.2-qter);Clinical Genetics;2008-06-28
5. Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features;American Journal of Medical Genetics Part A;2006
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